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临床试验/NCT01988155
NCT01988155已完成不适用

Eccentric Exercise Versus Eccentric Exercise and Astym® in the Management of Insertional Achilles Tendinopathy: A Randomized Controlled Trial

Indiana University Health Ball Memorial Hospital Rehabiliation Services1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2013年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
16
试验地点
1
主要终点
Victorian Institute of Sport Assessment- Achilles Specific Questionnaire (VISA-A)

研究概览

简要总结

The purpose of this research study is to determine if Astym® treatment is an effective treatment for patients with Achilles pain. The usual treatment for this condition is a specific exercise program that has been previously shown to be effective. The research team is trying to determine if combining Astym with the exercise program is more effective than exercise program only.

The main hypothesis for this study is that Astym plus eccentric exercise will be more effective than eccentric exercise alone at improving pain and function in patients with insertional Achilles tendinopathy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •diagnosis of insertional AT as a primary complaint*
  • •symptom duration of at least 6 weeks
  • •VISA-A score of 78 or lower
  • •he presence of insertional AT will be clinically determined by the primary investigator using the following criteria: pain at or within 2 cm of the posterior calcaneal insertion of the Achilles tendon along with localized tenderness and a subjective report of decreased activity levels secondary to Achilles pain.

排除标准

  • •prior treatment with eccentric exercise or Astym for Achilles tendinopathy
  • •currently taking anticoagulant medication
  • •usage of fluoroquinolone antibiotics in the previous six months
  • •previous Achilles surgery on the involved side
  • •bilateral symptoms
  • •pregnancy
  • •worker's compensation or liability cases
  • •peripheral neuropathy
  • •signs of lumbar radiculopathy
  • •inability to complete the required outcomes forms or comply with the recommended treatment regimen

研究组 & 干预措施

Eccentric Exericse

Active Comparator

干预措施: Eccentric Exercise (Other)

Astym

Experimental

干预措施: Astym (Other)

结局指标

主要结局

Victorian Institute of Sport Assessment- Achilles Specific Questionnaire (VISA-A)

时间窗: 12 weeks

次要结局

  • Numeric Pain Rating Scale (NPRS)(12 weeks)
  • Global Rating of Change Score (GROC)(12 weeks)

研究者

发起方
Indiana University Health Ball Memorial Hospital Rehabiliation Services
申办方类型
Other
责任方
Principal Investigator
主要研究者

Joshua McCormack

Physical Therapist

Indiana University Health Ball Memorial Hospital Rehabiliation Services

研究点 (1)

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